Reynier P - Search Results

1

Reversible optic neuropathy with OPA1 exon 5b mutation.

Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C, Reynier P, Lenaers G. Cornille K, et al. Among authors: reynier p. Ann Neurol. 2008 May;63(5):667-71. doi: 10.1002/ana.21376. Ann Neurol. 2008. PMID: 18360822 Free article.

2

Mitochondrial activity in XTC.UC1 cells derived from thyroid oncocytoma.

Savagner F, Chevrollier A, Loiseau D, Morgan C, Reynier P, Clark O, Stepien G, Malthiery Y. Savagner F, et al. Among authors: reynier p. Thyroid. 2001 Apr;11(4):327-33. doi: 10.1089/10507250152039055. Thyroid. 2001. PMID: 11349830

3

Oxygen consumption and expression of the adenine nucleotide translocator in cells lacking mitochondrial DNA.

Loiseau D, Chevrollier A, Douay O, Vavasseur F, Renier G, Reynier P, Malthièry Y, Stepien G. Loiseau D, et al. Among authors: reynier p. Exp Cell Res. 2002 Aug 1;278(1):12-8. doi: 10.1006/excr.2002.5553. Exp Cell Res. 2002. PMID: 12126953

4

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.

Funalot B, Reynier P, Vighetto A, Ranoux D, Bonnefont JP, Godinot C, Malthièry Y, Mas JL. Funalot B, et al. Among authors: reynier p. Ann Neurol. 2002 Sep;52(3):374-7. doi: 10.1002/ana.10299. Ann Neurol. 2002. PMID: 12205655

5

The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene.

Amati-Bonneau P, Odent S, Derrien C, Pasquier L, Malthiéry Y, Reynier P, Bonneau D. Amati-Bonneau P, et al. Among authors: reynier p. Am J Ophthalmol. 2003 Dec;136(6):1170-1. doi: 10.1016/s0002-9394(03)00665-2. Am J Ophthalmol. 2003. PMID: 14644237

6

Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.

Baris O, Delettre C, Amati-Bonneau P, Surget MO, Charlin JF, Catier A, Derieux L, Guyomard JL, Dollfus H, Jonveaux P, Ayuso C, Maumenee I, Lorenz B, Mohammed S, Tourmen Y, Bonneau D, Malthièry Y, Hamel C, Reynier P. Baris O, et al. Among authors: reynier p. Hum Mutat. 2003 Jun;21(6):656. doi: 10.1002/humu.9152. Hum Mutat. 2003. PMID: 14961560

7

Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1.

Amati-Bonneau P, Pasquier L, Lainey E, Ferré M, Odent S, Malthièry Y, Bonneau D, Reynier P. Amati-Bonneau P, et al. Among authors: reynier p. Clin Genet. 2005 Jan;67(1):102-3. doi: 10.1111/j.1399-0004.2004.00358.x. Clin Genet. 2005. PMID: 15617556 No abstract available.

8

Mitochondrial diseases preferentially involve proteins with prokaryote homologues.

Tourmen Y, Ferré M, Malthièry Y, Dessen P, Reynier P. Tourmen Y, et al. Among authors: reynier p. C R Biol. 2004 Dec;327(12):1095-101. doi: 10.1016/j.crvi.2004.09.005. C R Biol. 2004. PMID: 15656352 Free article.

9

eOPA1: an online database for OPA1 mutations.

Ferré M, Amati-Bonneau P, Tourmen Y, Malthièry Y, Reynier P. Ferré M, et al. Among authors: reynier p. Hum Mutat. 2005 May;25(5):423-8. doi: 10.1002/humu.20161. Hum Mutat. 2005. PMID: 15832306

10

[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs].

Verny C, Amati-Bonneau P, Dubas F, Malthiéry Y, Reynier P, Bonneau D. Verny C, et al. Among authors: reynier p. Rev Neurol (Paris). 2005 Apr;161(4):451-4. doi: 10.1016/s0035-3787(05)85075-1. Rev Neurol (Paris). 2005. PMID: 15924081 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

347 results

Search Page

Filters